Evidence map›Paper›PMID 32680576›Full record

ArticleJournal of nanobiotechnology2020

"Oil-soluble" reversed lipid nanoparticles for oral insulin delivery.

Tao Wang, Liao Shen, Yadan Zhang, Haiyan Li, Yongan Wang, Dongqin Quan

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Review
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  9. Article
  10. Interactions between Nanoparticles and Intestine.International journal of molecular sciences · 2022
    Review
  11. Article
  12. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Tao WangState Key Laboratory of Toxicology and Medical Countermeasure, Beijing Institute of Pharmacology and Toxicology, Beijing, 100850, China.
Liao ShenState Key Laboratory of Toxicology and Medical Countermeasure, Beijing Institute of Pharmacology and Toxicology, Beijing, 100850, China.
Yadan ZhangState Key Laboratory of Toxicology and Medical Countermeasure, Beijing Institute of Pharmacology and Toxicology, Beijing, 100850, China.
Haiyan LiState Key Laboratory of Toxicology and Medical Countermeasure, Beijing Institute of Pharmacology and Toxicology, Beijing, 100850, China.
Yongan WangState Key Laboratory of Toxicology and Medical Countermeasure, Beijing Institute of Pharmacology and Toxicology, Beijing, 100850, China. yonganw@126.com.
Dongqin QuanState Key Laboratory of Toxicology and Medical Countermeasure, Beijing Institute of Pharmacology and Toxicology, Beijing, 100850, China. qdqwzb@163.com.ORCID http://orcid.org/0000-0002-7767-5175

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn this study, we aimed to design a novel oral insulin delivery system, named "oil-soluble" reversed lipid nanoparticles (ORLN), in which a hydrophilic insulin molecule is encapsulated by a phospholipid (PC) shell and dissolved in oil to prevent the enzymatic degradation of insulin. ORLN was characterized by transmission electron microscopy and dynamic light scattering.

resultsIn vitro enzymatic stability studies showed higher concentrations of insulin in cells incubated with ORLN-encapsulated insulin than in those incubated with free insulin solution in artificial intestinal fluid (pH 6.5). The protective effect of ORLN was attributed to its special release behavior and the formulation of the PC shell and oil barrier. Furthermore, an in vivo oral efficacy study confirmed that blood glucose levels were markedly decreased after ORLN administration in both healthy and diabetic mice. In vivo pharmacokinetic results showed that the bioavailability of ORLN-conjugated insulin was approximately 28.7% relative to that of the group subcutaneously administered with an aqueous solution of insulin, indicating enhanced oral absorption.

conclusionsIn summary, the ORLN system developed here shows promise as a nanocarrier for improving the oral absorption of insulin.

Indexed as

Drug CarriersInsulinNanoparticlesAdministration, OralAnimalsBiological AvailabilityBlood GlucoseDiabetes Mellitus, ExperimentalHypoglycemic AgentsMaleMicePhospholipidsRats, WistarSolubilityBlood GlucoseDrug CarriersHypoglycemic AgentsInsulinPhospholipidsInsulinNanocarriers“Oil-soluble” reversed lipid nanoparticlesOral absorptionPhospholipid

Identifiers

PMID32680576
PMCPMC7367322

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.